US3850244A - Polymer flooding process - Google Patents
Polymer flooding process Download PDFInfo
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- US3850244A US3850244A US00369641A US36964173A US3850244A US 3850244 A US3850244 A US 3850244A US 00369641 A US00369641 A US 00369641A US 36964173 A US36964173 A US 36964173A US 3850244 A US3850244 A US 3850244A
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- 229920000642 polymer Polymers 0.000 title claims abstract description 100
- 238000000034 method Methods 0.000 title claims description 45
- 230000008569 process Effects 0.000 title claims description 43
- 239000000243 solution Substances 0.000 claims abstract description 61
- 230000035699 permeability Effects 0.000 claims abstract description 38
- 229920002401 polyacrylamide Polymers 0.000 claims abstract description 27
- 239000011435 rock Substances 0.000 claims abstract description 20
- 230000009467 reduction Effects 0.000 claims abstract description 16
- 238000002347 injection Methods 0.000 claims abstract description 14
- 239000007924 injection Substances 0.000 claims abstract description 14
- 229920001222 biopolymer Polymers 0.000 claims abstract description 13
- 230000000694 effects Effects 0.000 claims abstract description 12
- 229920001577 copolymer Polymers 0.000 claims abstract description 7
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 claims abstract description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229940047670 sodium acrylate Drugs 0.000 claims abstract description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 44
- 239000004215 Carbon black (E152) Substances 0.000 claims description 21
- 229930195733 hydrocarbon Natural products 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 20
- 150000002430 hydrocarbons Chemical class 0.000 claims description 17
- 239000011148 porous material Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 239000012530 fluid Substances 0.000 claims description 7
- 150000004676 glycans Chemical class 0.000 claims description 5
- 229920001282 polysaccharide Polymers 0.000 claims description 5
- 239000005017 polysaccharide Substances 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 3
- 230000006872 improvement Effects 0.000 claims description 3
- 238000006073 displacement reaction Methods 0.000 claims description 2
- 230000002349 favourable effect Effects 0.000 claims 2
- 238000011084 recovery Methods 0.000 abstract description 8
- 230000008859 change Effects 0.000 abstract description 2
- 239000007864 aqueous solution Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000009826 distribution Methods 0.000 description 3
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229920001897 terpolymer Polymers 0.000 description 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical group NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- XXAXVMUWHZHZMJ-UHFFFAOYSA-N Chymopapain Chemical compound OC1=CC(S(O)(=O)=O)=CC(S(O)(=O)=O)=C1O XXAXVMUWHZHZMJ-UHFFFAOYSA-N 0.000 description 1
- 108090001069 Chymopapain Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000801924 Sena Species 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- -1 hydroxy amines Chemical class 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
- C09K8/588—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids characterised by the use of specific polymers
Definitions
- ABSTRACT Mobility control is improved in secondary-type oil recovery through injection of two aqueous polymer solutions.
- the first solution effects permeability reduction and no fraction of the polymer deviates more than 5 percent from the average molecular weight polymer injected
- the second solution contains a polymer which does not substantially change rock permeability, but imparts a viscosity increase to the solution.
- An example of the polymer used in the first solution is a partially hydrolyzed polyacrylarnide or a copolymer of acrylamide and sodium acrylate or acrylic acid and in the second solution is a biopolymer.
- the second solution comprises a polymer having a substantially uniform molecular weight distribution and a high enough molecular weight to effect a substantial permeability reduction.
- the second solution comprises a polymer having properties which will impart increased viscosity without substantially affecting formation permeability. Essentially all of the polymer of the first aqueous polymer solution is effective in reducing formation permeability. This aqueous polymer solution will prevent denudation of the subsequent viscosity increasing polymer solutions by satisfying polymer loss occurring by sorption, e.g. adsorption, entrapment. etc. in the formation rock.
- the second aqueous polymer solution maintains mobility control by viscosity alone with little loss of the polymer due to mechanical entrapment. Applicants, combination is an economical and effective method of obtaining improved mobility I control and improving oil recoveries in'secondary type recovery processes.
- copolymers, terpolymers, etc. and chemically modified and/or chemically substituted (inorganic and/or organic substituted groups) products thereof.
- the polymers can have average molecular weights within the range of 500,000 to about 30,000,000 or more, prefer- 3,497,006 to Jones et al., 3,506,070 and 3,506,071 to Jones.
- the frontal portion of the waterflood has a mobility equal to or less than that of the fluids being displaced from the reservoir. Thereafter, the mobility of the waterflood is gradually increased until it is equal to that of water.
- Mobility control in a formation flooding process can be obtained by reducing the permeability to the flow of specific fluids through the formation and/or by increasing the viscosity of fluids flowing through the formation.
- a currently accepted practice is to incorporate into a waterflood a single agent, e.g. a partially hydrolyzed, high molecular weight polyacrylamide, to effect mobility control.
- the injection of a single mobility decreasing polymer is inefficient.
- These polymers typically have broad molecular weight distributions, and, as a result, only a small fraction of the polymer may be useful to effectively reduce formation permeability. This fraction may typically be ten percent (or less) of the total polymer present.
- Applicants have discovered a method of improving mobility control of a flooding process by injecting at least two separate aqueous polymer solutions.
- the first preferably about 1,000,000 to about 25,000,000 and more preferably about 5,000,000 to about 20,000,000.
- the molecular weight used depends upon the permeability and rock properties of the reservoir to be flooded.
- Especially useful polymers are the polyacrylamides having about 10-70 percent of the carboxy amide groups hydrolyzed to carboxyl groups, e. g. fractioniated Pusher polymers (Pusher is a trademark of Dow Chemical Company, Midland, Michigan, USA), the Puser polymers are defined in US. Pat. No. 2,827,964 to Sandiford et al and US. Pat. No.
- the polymer solution should contain a substantially uniform molecular weight polymer designed'for the properties of the specific formation rock with essentially no fraction deviating more than five per cent from the average molecular weight of the polymer in the aqueous polymer solution.
- the average molecular weight of the polymer within the first solution must be high enough to substantially reduce the permeability of the formation rock to the flow of aqueous solutions. Also, it must be low enough so as not tocompletely plug the formation and thereby decrease injectivity.
- polymer for a specific formation should be designed so that the average molecular weight is higher for formation rock exhibiting high permeability to the flow of aqueous solutions or lower for formation rock which exhibits lower permeability to the flow of aqueous solutions. For example, if the average permeability isabove about 150 md,
- the average molecular weight is preferably greater than about 10,000,000 but if the average permeability is about 25 to about md, then the average molecular weight of the polymer preferably is about 500,000 to about 10,000,000.
- the polymer within the first solution may be present in concentrations of about 50 to about 5,000 ppm, more preferably about 75 to about 3,000 ppm and most preferably about 100 to about 2,000 ppm.
- Polymers of the second solution useful as viscosity increasing agents include biopolymers, homopolymers, copolymers, terpolymers, etc., and chemically modifled and/or chemically substituted (inorganic and/or organic groups) products thereof.
- Molecular weights of these polymers can be about 500,000 to about 25,000,000, preferably about 750,000 to about 10,000,000 and more preferably about 1,000,000 to about 3,500,000. Again, the desired molecular weight is dependent upon the properties of the specific formation. The properties of these polymers should not permit a substantial reduction in permeability of the reservoir rock.
- Preferred polymers are biopolymers including polysaccharides and their derivatives (e.g. Kelzan- MF, a polysaccharide polymer marketed by the Xanco Division of Kelco Chemical Co., San Diego, California,
- the polymer of the second solution may be present in concentrations of about to about 5,000 ppm, more preferably about to about 3,000 ppm and most preferably about to about 2,000 ppm.
- the second solution may be injected in quantities of about 1 to about 500 percent formation pore volume, more preferably about 5 to about 200 percent formation pore volume and most preferably about 10 to about 100 percent formation pore volume.
- a flooding agent such as a miscible agent, a miscible-like agent, a hydrocarbon or water solubilizing agent, an immiscible agent or any other agent which tends to reduce interfacial tension between oil and water within the formation, may be useful with the invention.
- These agents are preferably injected prior to the injection of the aqueous polymer solutions.
- Examples of such flooding agents include oiland water- 7 external emulsions, oiland water-external micellar dis- Case L About pore volumes of polymer solution containing 500 ppm bioplymer (Kelzan MP) is injected at a constant rate of 2 ft/day.
- a reciprocal mobility of 5.2 cp is realized through a permeability reduction of 2.6 and an effective viscosity of 2.00 cp.
- Case 11 Same as case 1 except 5 pore volumes of 500 ppm partially hydrolyzed polyacrylamide (intrinsic viscosity of about 1 1 dl/gm in a 2 N sodium chloride solution) is injected.
- a reciprocal mobility of 15.2 cp is realized through a permeability reduction of 10.9 and an effective viscosity of 1.40 cp.
- Case 111 Same as Case 1 and 11 except 2 pore volumes of 500 ppm partially hydrolyzed polyacrylamide are first injected followed by 3 pore volumes of 250 ppm biopolymer.
- the highest reciprocal mobility (19.5 cp) is realized by the higher permeability reduction of the polyacrylamide and the higher effective viscosity of biopolymer with less total polymer injected.
- EXAMPLE ll Similar to Example 1 except md Illinois sandstone cores are used. Polymer l is a polyacrylamide copolymer (intrinsic viscosity 19.8 dl/g) and polymer 2 is an N-sulfohydrocarbon substituted acrylamide homopolymer (intrinsic viscosity 13.4 dl/g). Improvements similar to Example I are effected.
- polymer within the first solution is a partially hydrolyzed, high molecular weight polyacrylamide or copolymer of acrylamide and sodium acrylate or acrylic acid.
- biopolymer is a polysaccharide
- miscible. flooding agent is a micellar dispersion
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- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mining & Mineral Resources (AREA)
- Geology (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Fluid Mechanics (AREA)
- Physics & Mathematics (AREA)
- Geochemistry & Mineralogy (AREA)
- Environmental & Geological Engineering (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
Mobility control is improved in secondary-type oil recovery through injection of two aqueous polymer solutions. The first solution effects permeability reduction and no fraction of the polymer deviates more than 5 percent from the average molecular weight polymer injected. The second solution contains a polymer which does not substantially change rock permeability, but imparts a viscosity increase to the solution. An example of the polymer used in the first solution is a partially hydrolyzed polyacrylamide or a copolymer of acrylamide and sodium acrylate or acrylic acid and in the second solution is a biopolymer.
Description
FIR/912 OR Nov. 26, 1974 POLYMER FLOODING PROCESS [75] Inventors; John S. Rhudy; William B. Gogarty;
Bruce L. Knight, all of Littleton;
, James H. Fullinwider, Aurora, all of Colo.
[73] Assignee: Marathon Oil Company, Findlay,
Ohio
[22] Filed: June 13, 1973 [21] Appl. No.: 369,641
[52] U.S. Cl. 166/273, 166/274 [51] Int. Cl E2lb 43/22 [58] Field of Search 166/273, 274, 252; 252/8.55 D
[56] References Cited UNITED STATES PATENTS 3,724,545 4/1973 Knight 166/273 Primary Examiner-Stephen J. Novosad Attorney, Agent, or FirmJoseph C. Herring; Richard C. Willson, Jr.; Jack L. Hummel [57] ABSTRACT Mobility control is improved in secondary-type oil recovery through injection of two aqueous polymer solutions. The first solution effects permeability reduction and no fraction of the polymer deviates more than 5 percent from the average molecular weight polymer injected The second solution contains a polymer which does not substantially change rock permeability, but imparts a viscosity increase to the solution. An example of the polymer used in the first solution is a partially hydrolyzed polyacrylarnide or a copolymer of acrylamide and sodium acrylate or acrylic acid and in the second solution is a biopolymer.
19 Claims, N0 Drawings BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to injecting at least two fluids through an injection well in fluid communication with a hydrocarbon-bearing subterranean formation and displacing them toward a production well to recover hydrocarbon therethrough.
2. Description of the Prior Art Improved recoveries of hydrocarbon in secondary recovery operations have been obtained by waterflooding with mobility reducing agents. US. Pat. No. 3,039,529 to McKennon teaches that about 100 to about 5,000 ppm of a high molecular weight, partially hydrolyzed polyacrylamide is useful for this purpose. US. Pat. No. 2,771,138 to Beeson uses naturally occurring gums and polymers, aqueous solutions containing synthetic polymers, e.g. copolymers of methylvinyl ether and maleic anhydride, condensation products of fatty acids and hydroxy amines, sodium polyacrylate, polyacrylic acid, sodium polymethacrylate, etc., sucrose and crude sugar, etc., as viscosityincreasing agents in waterflooding processes. Improved mobility control has also been obtained using a mobility buffer slug behind a miscible or miscible-like displacing agent, e.g. see US. Pat. Nos. 3,254,714 to Gogarty et al.,
solution comprises a polymer having a substantially uniform molecular weight distribution and a high enough molecular weight to effect a substantial permeability reduction. The second solution comprises a polymer having properties which will impart increased viscosity without substantially affecting formation permeability. Essentially all of the polymer of the first aqueous polymer solution is effective in reducing formation permeability. This aqueous polymer solution will prevent denudation of the subsequent viscosity increasing polymer solutions by satisfying polymer loss occurring by sorption, e.g. adsorption, entrapment. etc. in the formation rock. The second aqueous polymer solution maintains mobility control by viscosity alone with little loss of the polymer due to mechanical entrapment. Applicants, combination is an economical and effective method of obtaining improved mobility I control and improving oil recoveries in'secondary type recovery processes.
DESCRIPTION OF PREFERRED EMBODIMENTS Polymers particularly useful to effect permeability reduction are thesynthesized organic homopolymers,
. copolymers, terpolymers, etc. and chemically modified and/or chemically substituted (inorganic and/or organic substituted groups) products thereof. The polymers can have average molecular weights within the range of 500,000 to about 30,000,000 or more, prefer- 3,497,006 to Jones et al., 3,506,070 and 3,506,071 to Jones.
The prior art generally'teaches that optimal mobility conditions, e.g. less fingering and therefore improved oil recovery, are obtained when the leading portion of the waterflood contains a viscosity increasing agent. It
is preferable that the frontal portion of the waterflood has a mobility equal to or less than that of the fluids being displaced from the reservoir. Thereafter, the mobility of the waterflood is gradually increased until it is equal to that of water.
Mobility control in a formation flooding process can be obtained by reducing the permeability to the flow of specific fluids through the formation and/or by increasing the viscosity of fluids flowing through the formation. A currently accepted practice is to incorporate into a waterflood a single agent, e.g. a partially hydrolyzed, high molecular weight polyacrylamide, to effect mobility control. The injection of a single mobility decreasing polymer, however, is inefficient. These polymers typically have broad molecular weight distributions, and, as a result, only a small fraction of the polymer may be useful to effectively reduce formation permeability. This fraction may typically be ten percent (or less) of the total polymer present. When this permeability reducing fraction has been deposited on the rock matrix, mobility control by increased viscosity is minimal because of the low effective viscosity of the remaining polymer. Or, if the molecular weight distribution is too broad and the average molecular weight too high, the permeability and injectivity may be reduced too much to permit efficient oil recovery. Thus, obtaining improved mobility control through the use of a single polymer is inefficient and can be ineffective.
SUMMARY OF THE INVENTION Applicants have discovered a method of improving mobility control of a flooding process by injecting at least two separate aqueous polymer solutions. The first ably about 1,000,000 to about 25,000,000 and more preferably about 5,000,000 to about 20,000,000. The molecular weight used depends upon the permeability and rock properties of the reservoir to be flooded. Especially useful polymers are the polyacrylamides having about 10-70 percent of the carboxy amide groups hydrolyzed to carboxyl groups, e. g. fractioniated Pusher polymers (Pusher is a trademark of Dow Chemical Company, Midland, Michigan, USA), the Puser polymers are defined in US. Pat. No. 2,827,964 to Sandiford et al and US. Pat. No. 3,039,529 to McKennon. Other examples of useful polymers are defined in US. Pat. No. 2,842,492 to Engelhardt et al; 3,282,337 and 3,399,725 to Pye; and 3,679,000 to Kaufman. Sulfonated alkyl derivatives of acrylamide are also useful.
Any polymer which'effectively reduce the permeability of the formation rock to the flow of aqueous solution may be used with the present invention. The polymer solution should contain a substantially uniform molecular weight polymer designed'for the properties of the specific formation rock with essentially no fraction deviating more than five per cent from the average molecular weight of the polymer in the aqueous polymer solution. The average molecular weight of the polymer within the first solution must be high enough to substantially reduce the permeability of the formation rock to the flow of aqueous solutions. Also, it must be low enough so as not tocompletely plug the formation and thereby decrease injectivity. Thus, polymer for a specific formation should be designed so that the average molecular weight is higher for formation rock exhibiting high permeability to the flow of aqueous solutions or lower for formation rock which exhibits lower permeability to the flow of aqueous solutions. For example, if the average permeability isabove about 150 md,
the average molecular weight is preferably greater than about 10,000,000 but if the average permeability is about 25 to about md, then the average molecular weight of the polymer preferably is about 500,000 to about 10,000,000. The polymer within the first solution may be present in concentrations of about 50 to about 5,000 ppm, more preferably about 75 to about 3,000 ppm and most preferably about 100 to about 2,000 ppm.
Polymers of the second solution useful as viscosity increasing agents include biopolymers, homopolymers, copolymers, terpolymers, etc., and chemically modifled and/or chemically substituted (inorganic and/or organic groups) products thereof. Molecular weights of these polymers can be about 500,000 to about 25,000,000, preferably about 750,000 to about 10,000,000 and more preferably about 1,000,000 to about 3,500,000. Again, the desired molecular weight is dependent upon the properties of the specific formation. The properties of these polymers should not permit a substantial reduction in permeability of the reservoir rock. Preferred polymers are biopolymers including polysaccharides and their derivatives (e.g. Kelzan- MF, a polysaccharide polymer marketed by the Xanco Division of Kelco Chemical Co., San Diego, California,
U.S.A.); see U.S. Pat. No. 3,305,016 to Lindblom for a description of biopolymers. Also useful are watersoluble, linear, high molecular weight monoalkyl argpersions, hydrocarbon and/or water containing surfactants, alcohols, electrolytes, and like components or mixtures thereof. Uses of flooding agents are taught in U.S. Pat. No. 3,254,714 to Gogarty et al; U.S. Pat. No. 3,307,628 to Sena; U.S. Pat. No. 3,356,138 to Davis, Jr. et a1; U.S. Pat. No. 3,376,925 to Coppel; U.S. Pat. No. 3,406,754 to Gogarty; U.S. Pat. No; 3,348,611 and U.S. Pat. No. 3,330,343 to Reisberg; U.S. Pat. No.
3,354,953 to Morse; U.S. Pat. Nos. 3,373,809 and EXAMPLE I Sandstone cores having permeabilities of about 80 md are cleaned and then saturated with water. The cores are flooded with polymer solutions described in Table 1:
TABLE 1 FLOODlNG RESULTS Reciprocal Flushed Permeability Mobility Permeability Permeability Effective Polymer (md) llcp) (md) Reduction Viscosity Case I 5 pore volumes 74 5.2 $18 2.6 2.00
500 ppm of Kelzan MF Case 11 5 pore volumes 78 15.2 7.2 10.9 1.40
500 ppm of partially hydrolyzed polyacrylamide Case lll 2 pore volumes 86 19.5 7.9 10.9 1.79
500 ppm partially hydrolyzed polyacrylamide followed by 3 pore volumes of 250 ppm Kelzan MF matic sulfonate polymers as to Kaufman (N-sulfohydrocarbon substituted acrylamide polymers). The polymer of the second solution may be present in concentrations of about to about 5,000 ppm, more preferably about to about 3,000 ppm and most preferably about to about 2,000 ppm. The second solution may be injected in quantities of about 1 to about 500 percent formation pore volume, more preferably about 5 to about 200 percent formation pore volume and most preferably about 10 to about 100 percent formation pore volume.
A flooding agent, such as a miscible agent, a miscible-like agent, a hydrocarbon or water solubilizing agent, an immiscible agent or any other agent which tends to reduce interfacial tension between oil and water within the formation, may be useful with the invention. These agents are preferably injected prior to the injection of the aqueous polymer solutions. Examples of such flooding agents include oiland water- 7 external emulsions, oiland water-external micellar dis- Case L About pore volumes of polymer solution containing 500 ppm bioplymer (Kelzan MP) is injected at a constant rate of 2 ft/day. A reciprocal mobility of 5.2 cp is realized through a permeability reduction of 2.6 and an effective viscosity of 2.00 cp. Case 11. Same as case 1 except 5 pore volumes of 500 ppm partially hydrolyzed polyacrylamide (intrinsic viscosity of about 1 1 dl/gm in a 2 N sodium chloride solution) is injected. A reciprocal mobility of 15.2 cp is realized through a permeability reduction of 10.9 and an effective viscosity of 1.40 cp.
Case 111. Same as Case 1 and 11 except 2 pore volumes of 500 ppm partially hydrolyzed polyacrylamide are first injected followed by 3 pore volumes of 250 ppm biopolymer.
The highest reciprocal mobility (19.5 cp) is realized by the higher permeability reduction of the polyacrylamide and the higher effective viscosity of biopolymer with less total polymer injected.
EXAMPLE ll Similar to Example 1 except md Illinois sandstone cores are used. Polymer l is a polyacrylamide copolymer (intrinsic viscosity 19.8 dl/g) and polymer 2 is an N-sulfohydrocarbon substituted acrylamide homopolymer (intrinsic viscosity 13.4 dl/g). Improvements similar to Example I are effected.
What is claimed is: 1. In a process of recovering hydrocarbon from a hydrocarbon-bearing subterranean formation having at least one injection means in fluid communication with at least one production means and wherein polymer solution is injected into the formation to displace hydrocarbon toward the production means through which hydrocarbon is recovered, the improvement comprising injecting a first solution comprised of substantially uniform molecular weight polymer of sufficient. concentration and sufficient molecular weight to' substantially effect permeability reduction of the formation rock, and then injecting a second solution comprised of a polymer that will not substantially effect further permeability reduction of the formation rock h lii fii ififi llpflym f scncsntretiq zm mp rtincreased viscosity to the polymer solution for more fa vorable mobility control in the displacement of hydrocarbon from the formation.
2. The process of claim 1 wherein the average molecular weight of the polymer within the first solution is greater than about 10,000,000 and the average permeability of the formation rock is above about 150 md.
3. The process of claim 1 wherein the polymer within the first solution is a partially hydrolyzed, high molecular weight polyacrylamide or copolymer of acrylamide and sodium acrylate or acrylic acid.
4. The process of claim 3 wherein the polyacrylamide is present at a concentration of about 100 to about 2,000 ppm.
5. The process of claim 1 wherein the polymer within the second solution is a partially hydrolyzed, high molecular weight polyacrylamide.
6. The process of claim 5 wherein the polyacrylamide has a molecular weight of about 500,000 to about 10,000,000.
7. The process of claim 5 wherein the concentration of polyacrylamide is about 100 to about 2,000 ppm.
8. The process of claim 1 wherein the polymer within the second solution is a biopolymer.
9. The process of claim 8 wherein the biopolymer is a polysaccharide.
10. The process of claim 1 wherein the polymer within the second solution is an N-sulfohydrocarbon substituted acrylamide polymer.
11. The process of claim 1 wherein the injection of the first solution is preceded by an injection of a miscible or miscible-like flooding agent.
12. The process of claim 11 wherein the miscible. flooding agent is a micellar dispersion,
13. An improved process for effecting mobility control in a process for recovering hydrocarbon from a hydrocarbon-bearing formation wherein an aqueous polymer solution is injected into the formation through an injection means and displaced toward a production means to recover hydrocarbon therethrough and wherein the formation rock has an average permeability of at least about 25 md, the improved process comprising:
l. injecting about 5 to about percent formation pore volume of a first aqueous polymer solution containing'a polymer having a substantially uniform molecular weight within the range of about 500,000 to about 30,000,000, uniform molecular weight being defined as having substantially no fraction of the polymer which deviates more than about 5 percent from the average molecular weight of the polymer, and being sufficient molecular weight and sufficient concentration to effect permeability reduction of the formation rock, and
injecting about 10 to about percent formation pore volume of a second aqueous polymer solution containing a polymer having an average molecular weight of about 500,000 to about 10,000,000, the molecular weight not being high enough to substantially effect permeability reduction of the formation rock, and the polymer in sufficient concentration to impart favorablemobility control, and
3. displacing the aqueous polymer solutions of 1) and 2) toward the production means to recover hydrocarbon therethrough. 14. The process of claim 13 wherein the polymer within the aqueous polymer solution of step 1) is a partially hydrolyzed, high molecular weight polyacrylamide.
15. The process of claim 13 wherein the polymer
Claims (21)
1. IN A PROCESS OF RECOVERING HYDROCARBON FROM A HYDROCARBON-BEARING SUBTERRENEAN FORMATION HAVING AT LEAST ONE INJECTION MEANS IN FLUID COMMUNICATION WITH AT LEAST ONE PRODUCTION MEANS AND WHEREIN POLYMER SOLUTION IS INJECTED INTO THE FORMATION TO DISPLACE HYDROCARBON TOWARD THE PRODUCTION MEANS THROUGH WHICH HYDROCARBON IS RECOVERED, THE IMPROVEMENT COMPRISING INJECTING A FIRST SOLUTION COMPRISED OF A SUBSTANTIALLY UNIFRM MOLECULAR WEIGHT POLYMER OF SUFFICIENT CONCENTRATION AND SUFFICIENT MOLECULAR WEIGHT TO SUBSTANTIALLY EFFECT PERMEABILITY REDUCTION OF THE FORMATION ROCK, AND THEN INJECTING A SECOND SOLUTION COMPRISED OF A POLYMER THAT WILL NOT SUBSTANTIALLY EFFECT FURTHER PERMEABILITY REDUCTION OF THE FORMATION ROCK BUT OF A SUFFICIENT POLYMER CONCENTRATION TO IMPART INCREASED VISCOSITY TO THE POLYMER SOLUTION FOR MORE FAVORABLE MOBILITY CONTROL IN THE DISPLACEMENT OF HDROCARBON FROM THE FORMATION.
2. The process of claim 1 wherein the average molecular weight of the polymer within the first solution is greater than about 10,000,000 and the average permeability of the formation rock is above about 150 md.
2. injecting about 10 to about 100 percent formation pore volume of a second aqueous polymer solution containing a polymer having an average molecular weight of about 500,000 to about 10,000,000, the molecular weight not being high enough to substantially effect permeability reduction of the formation rock, and the polymer in sufficient concentration to impart favorable mobility control, and
3. displacing the aqueous polymer solutions of ''''1)'''' and ''''2)'''' toward the production means to recover hydrocarbon therethrough.
3. The process of claim 1 wherein the polymer within the first solution is a partially hydrolyzed, high molecular weight polyacrylamide or copolymer of acrylamide and sodium acrylate or acrylic acid.
4. The process of claim 3 wherein the polyacrylamide is present at a concentration of about 100 to about 2,000 ppm.
5. The process of claim 1 wherein the polymer within the second solution is a partially hydrolyzed, high molecular weight polyacrylamide.
6. The process of claim 5 wherein the polyacrylamide has a molecular weight of about 500,000 to about 10,000,000.
7. The process of claim 5 wherein the concentration of polyacrylamide is about 100 to about 2,000 ppm.
8. The process of claim 1 wherein the polymer within the second solutIon is a biopolymer.
9. The process of claim 8 wherein the biopolymer is a polysaccharide.
10. The process of claim 1 wherein the polymer within the second solution is an N-sulfohydrocarbon substituted acrylamide polymer.
11. The process of claim 1 wherein the injection of the first solution is preceded by an injection of a miscible or miscible-like flooding agent.
12. The process of claim 11 wherein the miscible flooding agent is a micellar dispersion.
13. An improved process for effecting mobility control in a process for recovering hydrocarbon from a hydrocarbon-bearing formation wherein an aqueous polymer solution is injected into the formation through an injection means and displaced toward a production means to recover hydrocarbon therethrough and wherein the formation rock has an average permeability of at least about 25 md, the improved process comprising:
14. The process of claim 13 wherein the polymer within the aqueous polymer solution of step ''''1)'''' is a partially hydrolyzed, high molecular weight polyacrylamide.
15. The process of claim 13 wherein the polymer within the aqueous polymer solution of step ''''2)'''' is a biopolymer.
16. The process of claim 15 wherein the biopolymer is a polysaccharide.
17. The process of claim 13 wherein the polymer within the aqueous polymer solution of step ''''2)'''' is an N-sulfohydrocarbon substituted acrylamide polymer.
18. The process of claim 13 wherein step ''''1)'''' is preceded by an injection of a miscible or miscible-like flooding agent.
19. The process of claim 18 wherein the miscible-like flooding agent is a micellar dispersion.
Priority Applications (1)
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US00369641A US3850244A (en) | 1973-06-13 | 1973-06-13 | Polymer flooding process |
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US00369641A US3850244A (en) | 1973-06-13 | 1973-06-13 | Polymer flooding process |
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US3850244A true US3850244A (en) | 1974-11-26 |
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US00369641A Expired - Lifetime US3850244A (en) | 1973-06-13 | 1973-06-13 | Polymer flooding process |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3908764A (en) * | 1974-11-25 | 1975-09-30 | Phillips Petroleum Co | Method of treating petroleum-bearing formations for supplemental oil recovery |
US3945929A (en) * | 1974-05-08 | 1976-03-23 | Calgon Corporation | Process for the secondary or tertiary recovery of petroleum |
US3953342A (en) * | 1974-05-08 | 1976-04-27 | Calgon Corporation | Petroleum recovery process |
US4039028A (en) * | 1975-11-03 | 1977-08-02 | Union Oil Company Of California | Mobility control of aqueous fluids in porous media |
FR2420020A1 (en) * | 1978-03-17 | 1979-10-12 | Texaco Ag | OIL EXTRACTION PROCESS BY SUCCESSIVE INJECTIONS OF POLYMER SOLUTIONS |
US4195689A (en) * | 1978-11-06 | 1980-04-01 | Cities Service Company | Chemical waterflood process development |
US4540498A (en) * | 1983-05-31 | 1985-09-10 | The Standard Oil Company | Block copolymers for enhanced oil recovery |
US4586568A (en) * | 1985-08-29 | 1986-05-06 | Phillips Petroleum Company | Polymerflood process |
US4915174A (en) * | 1983-02-14 | 1990-04-10 | Rhone-Poulenc Specialites Chimiques | Concentrated suspensions of water soluble polymers |
CN103216211A (en) * | 2012-01-18 | 2013-07-24 | 中国石油天然气股份有限公司 | Profile control method for fractured reservoir |
RU2779501C1 (en) * | 2022-02-21 | 2022-09-08 | Общество с ограниченной ответственностью "Тюменский нефтяной научный центр" (ООО "ТННЦ") | Method for developing a geologically heterogeneous oil reservoir by waterflooding |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US3724545A (en) * | 1970-09-28 | 1973-04-03 | Marathon Oil Co | Economical mobility control in oil recovery processes |
-
1973
- 1973-06-13 US US00369641A patent/US3850244A/en not_active Expired - Lifetime
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US3724545A (en) * | 1970-09-28 | 1973-04-03 | Marathon Oil Co | Economical mobility control in oil recovery processes |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3945929A (en) * | 1974-05-08 | 1976-03-23 | Calgon Corporation | Process for the secondary or tertiary recovery of petroleum |
US3953342A (en) * | 1974-05-08 | 1976-04-27 | Calgon Corporation | Petroleum recovery process |
US3908764A (en) * | 1974-11-25 | 1975-09-30 | Phillips Petroleum Co | Method of treating petroleum-bearing formations for supplemental oil recovery |
US4039028A (en) * | 1975-11-03 | 1977-08-02 | Union Oil Company Of California | Mobility control of aqueous fluids in porous media |
US4282930A (en) * | 1978-03-17 | 1981-08-11 | Deutsche Texaco Aktiengesellschaft | Process for the recovery of petroleum from subterranean formations |
FR2420020A1 (en) * | 1978-03-17 | 1979-10-12 | Texaco Ag | OIL EXTRACTION PROCESS BY SUCCESSIVE INJECTIONS OF POLYMER SOLUTIONS |
US4195689A (en) * | 1978-11-06 | 1980-04-01 | Cities Service Company | Chemical waterflood process development |
US4915174A (en) * | 1983-02-14 | 1990-04-10 | Rhone-Poulenc Specialites Chimiques | Concentrated suspensions of water soluble polymers |
US4540498A (en) * | 1983-05-31 | 1985-09-10 | The Standard Oil Company | Block copolymers for enhanced oil recovery |
US4586568A (en) * | 1985-08-29 | 1986-05-06 | Phillips Petroleum Company | Polymerflood process |
CN103216211A (en) * | 2012-01-18 | 2013-07-24 | 中国石油天然气股份有限公司 | Profile control method for fractured reservoir |
CN103216211B (en) * | 2012-01-18 | 2015-09-23 | 中国石油天然气股份有限公司 | Profile control method for fractured reservoir |
RU2779501C1 (en) * | 2022-02-21 | 2022-09-08 | Общество с ограниченной ответственностью "Тюменский нефтяной научный центр" (ООО "ТННЦ") | Method for developing a geologically heterogeneous oil reservoir by waterflooding |
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Owner name: MARATHON OIL COMPANY, AN OH CORP Free format text: ASSIGNS THE ENTIRE INTEREST IN ALL PATENTS AS OF JULY 10,1982 EXCEPT PATENT NOS. 3,783,944 AND 4,260,291. ASSIGNOR ASSIGNS A FIFTY PERCENT INTEREST IN SAID TWO PATENTS AS OF JULY 10,1982;ASSIGNOR:MARATHON PETROLEUM COMPANY;REEL/FRAME:004172/0421 Effective date: 19830420 |